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6479008: Partial albinism (disorder)

SNOMED CT Concept\Clinical finding\Disease\...

\Genetic disease\Hereditary disease\...

\Hereditary metabolic disease\Inborn error of metabolism\Albinism\Partial albinism

\Developmental hereditary disorder\Albinism\Partial albinism

\Disorder of pigmentation\Albinism\Partial albinism

\Metabolic disease\Hereditary metabolic disease\Inborn error of metabolism\Albinism\Partial albinism

\Congenital disease\Congenital malformation\Albinism\Partial albinism
\Congenital disease\Inborn error of metabolism\Albinism\Partial albinism

\Developmental disorder\Developmental hereditary disorder\Albinism\Partial albinism
\Developmental disorder\Congenital malformation\Albinism\Partial albinism

Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jan 2002. Module: SNOMED CT core module

Descriptions:

Id Description Lang Type Status Case? Module

11747017 Partial albinism en Synonym Active Entire term case insensitive SNOMED CT core module

804222017 Partial albinism (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core module

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Partial albinism	Is a	Albinism	true	Inferred relationship	Existential restriction modifier
Partial albinism	Finding site	Structure of skin region	false	Inferred relationship	Existential restriction modifier	1
Partial albinism	Finding site	Skin structure	false	Inferred relationship	Existential restriction modifier	3
Partial albinism	Associated morphology	Congenital hypopigmentation	false	Inferred relationship	Existential restriction modifier	1
Partial albinism	Finding site	Structure of eye proper	false	Inferred relationship	Existential restriction modifier
Partial albinism	Occurrence	Congenital	false	Inferred relationship	Existential restriction modifier
Partial albinism	Associated morphology	Congenital deficiency	false	Inferred relationship	Existential restriction modifier
Partial albinism	Finding site	Eye region structure	false	Inferred relationship	Existential restriction modifier
Partial albinism	Associated morphology	Congenital hypopigmentation	false	Inferred relationship	Existential restriction modifier
Partial albinism	Finding site	Structure of eye proper	false	Inferred relationship	Existential restriction modifier	2
Partial albinism	Associated morphology	Decreased melanin pigmentation	false	Inferred relationship	Existential restriction modifier
Partial albinism	Occurrence	Congenital	true	Inferred relationship	Existential restriction modifier	1
Partial albinism	Associated morphology	Congenital hypopigmentation	false	Inferred relationship	Existential restriction modifier	1
Partial albinism	Occurrence	Congenital	false	Inferred relationship	Existential restriction modifier	2
Partial albinism	Associated morphology	Decreased melanin pigmentation	false	Inferred relationship	Existential restriction modifier	2
Partial albinism	Associated morphology	Decreased melanin pigmentation	true	Inferred relationship	Existential restriction modifier	1
Partial albinism	Pathological process	Pathological developmental process	true	Inferred relationship	Existential restriction modifier	1
Partial albinism	Associated morphology	Hypopigmentation	false	Inferred relationship	Existential restriction modifier	1

Inbound Relationships	Type	Active	Source	Characteristic	Refinability	Group
Chédiak-Higashi syndrome	Is a	True	Partial albinism	Inferred relationship	Existential restriction modifier

This concept is not in any reference sets

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Id	Description	Lang	Type	Status	Case?	Module
11747017	Partial albinism	en	Synonym	Active	Entire term case insensitive	SNOMED CT core module
804222017	Partial albinism (disorder)	en	Fully specified name	Active	Entire term case insensitive	SNOMED CT core module